TY - JOUR
T1 - Subcellular localization of VDAC in mitochondria and ER in the cerebellum
AU - Shoshan-Barmatz, Varda
AU - Zalk, Ran
AU - Gincel, Dan
AU - Vardi, Noga
N1 - Funding Information:
This research was supported in part by grants from the Israel Science Foundation, administrated by The Israel Academy of Science to V.S-B., from NIH EY11105 to N.V and from NIH EY00828 to Peter Sterling, University of Pennsylvania (in whose lab portion of this work was carried out).
PY - 2004/7/9
Y1 - 2004/7/9
N2 - The voltage-dependent anion channel (VDAC) provides passage for adenine nucleotides, Ca2+ and other metabolites into and from mitochondria. Here, the intracellular localization and oligomeric organization of VDAC in brain mitochondria and ER are demonstrated. Immunohistochemical staining of VDAC in rat cerebellum showed high labeling of the Purkinje neurons. Immunogold labeling and EM analysis of the cerebellar molecular layer showed specific VDAC immunostaining of the mitochondrial outer membrane, highly enhanced in contact sites between mitochondria or between mitochondria and associated ER. Purified ER membranes contain VDAC, but not other mitochondrial proteins. Chemical cross-linking of isolated mitochondria, ER or purified VDAC demonstrated the existence of VDAC in oligomeric form. Based on the enrichment of VDAC in the junctional face of closely associated mitochondrial and ER membranes and the existence of VDAC oligomers, we propose an involvement of VDAC in specialized intermembrane communication between mitochondria or between ER and mitochondria, serving to complement the tight structural and functional coupling observed between these organelles.
AB - The voltage-dependent anion channel (VDAC) provides passage for adenine nucleotides, Ca2+ and other metabolites into and from mitochondria. Here, the intracellular localization and oligomeric organization of VDAC in brain mitochondria and ER are demonstrated. Immunohistochemical staining of VDAC in rat cerebellum showed high labeling of the Purkinje neurons. Immunogold labeling and EM analysis of the cerebellar molecular layer showed specific VDAC immunostaining of the mitochondrial outer membrane, highly enhanced in contact sites between mitochondria or between mitochondria and associated ER. Purified ER membranes contain VDAC, but not other mitochondrial proteins. Chemical cross-linking of isolated mitochondria, ER or purified VDAC demonstrated the existence of VDAC in oligomeric form. Based on the enrichment of VDAC in the junctional face of closely associated mitochondrial and ER membranes and the existence of VDAC oligomers, we propose an involvement of VDAC in specialized intermembrane communication between mitochondria or between ER and mitochondria, serving to complement the tight structural and functional coupling observed between these organelles.
KW - 3,3′-diamino-benzidine tetrahydrochloride
KW - Cerebellum
KW - DAB
KW - DMS
KW - DSP
KW - EGS
KW - EGTA
KW - ER and mitochondria
KW - VDAC
KW - dimethylsuberimidate
KW - dithiobis(succinimidylpropionate)
KW - ethylene glycol bis (aminoethylether) tetraacetate
UR - http://www.scopus.com/inward/record.url?scp=3242728582&partnerID=8YFLogxK
U2 - 10.1016/j.bbabio.2004.02.009
DO - 10.1016/j.bbabio.2004.02.009
M3 - Article
AN - SCOPUS:3242728582
SN - 0005-2728
VL - 1657
SP - 105
EP - 114
JO - Biochimica et Biophysica Acta - Bioenergetics
JF - Biochimica et Biophysica Acta - Bioenergetics
IS - 2-3
ER -